A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333950



Internal ID20867131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:176466960..176471503hg38UCSC Ensembl
chr1:176436096..176440639hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg384544
hg194544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053740
Samples
Known GenesPAPPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333950
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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